| Literature DB >> 31497212 |
Jiao Tang1, Jie Xu2, Zhongwen Zhi3, Xiang Wang3, Yu Wang4, Yong Zhou3, Rui Chen3.
Abstract
Aberrant expression of miRNAs has been reported to be involved in the development and progression of glioma. But the function of miR-876-3p in glioma is unknown. We found that miR-876-3p is significantly downregulated in glioma tissues and cell lines. Overexpression of miR-876-3p suppressed glioma cell proliferation, epithelial-mesenchymal transition, migration, and invasion. By prediction combining with luciferase reporter assay, we identified that miR-876-3p could decrease the expression of KIF20A by directly targeting the region of its 3'UTR. Furthermore, we observed that overexpression of miR-876-3p inhibited the expression of KIF20A, thus blocking the protein kinase JAK2/STAT3 pathway. Overexpressed KIF20A reversed miR-876-3p-induced suppression of glioma cell proliferation, migration, and invasion. We also demonstrated the inhibitory effect of miR-876-3p on tumor growth in glioma using an in vivo model. The miR-876-3p/KIF20A-axis mediated JAK2/STAT3 pathway have therapeutic potential in glioma treatment.Entities:
Keywords: EMT; Glioma; KIF20A; miR-876-3p; proliferation
Year: 2019 PMID: 31497212 PMCID: PMC6731397
Source DB: PubMed Journal: Am J Transl Res ISSN: 1943-8141 Impact factor: 4.060